TY  - RPRT
TI  - Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
AU  - Homburger, J. R.
AU  - Neben, C. L.
AU  - Mishne, G.
AU  - Zhou, A. Y.
AU  - Kathiresan, S.
AU  - Khera, A. V.
PY  - 2019
DO  - 10.1101/716977
UR  - https://www.biorxiv.org/content/10.1101/716977v1
ID  - 10.1101/716977
ER  -